Canonical Allele Identifier: CA10576178
Gene: VKORC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 225975
dbSNP Id: rs2359612

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31092475A>G , CM000678.2:g.31092475A>G GRCh38
NC_000016.9:g.31103796A>G , CM000678.1:g.31103796A>G GRCh37
NC_000016.8:g.31011297A>G NCBI36
NG_011564.1:g.7481T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000394975.3:c.283+837T>C MANE Select ENSP00000378426.2:n.283+837T>C
ENST00000300851.10:c.344+837T>C ENSP00000300851.6:n.344+837T>C
ENST00000319788.11:c.365+308T>C ENSP00000326135.7:n.365+308T>C
ENST00000354895.4:c.174-1133T>C ENSP00000346969.4:n.174-1133T>C
ENST00000394971.7:c.377+837T>C ENSP00000378422.3:n.377+837T>C
ENST00000394975.2:c.283+837T>C ENSP00000378426.2:n.283+837T>C
ENST00000420057.2:c.246-1133T>C
ENST00000472468.1:c.-33+837T>C ENSP00000458994.1:n.-33+837T>C
ENST00000498155.1:c.380+837T>C ENSP00000417662.1:n.380+837T>C
ENST00000529564.1:c.283+837T>C ENSP00000431371.1:n.283+837T>C
ENST00000532364.1:c.173+2082T>C ENSP00000460316.1:n.173+2082T>C
ENST00000533518.5:c.156+837T>C
NM_001311311.1:c.367+308T>C NP_001298240.1:n.367+308T>C
NM_024006.4:c.283+837T>C NP_076869.1:n.283+837T>C
NM_024006.5:c.283+837T>C NP_076869.1:n.283+837T>C
NM_206824.1:c.174-1133T>C NP_996560.1:n.174-1133T>C
NM_206824.2:c.174-1133T>C NP_996560.1:n.174-1133T>C
XM_011545944.1:c.283+837T>C XP_011544246.1:n.283+837T>C
XM_011545945.1:c.174-1133T>C XP_011544247.1:n.174-1133T>C
XR_950848.1:n.1071+837T>C
NM_024006.6:c.283+837T>C MANE Select NP_076869.1:n.283+837T>C
NM_001311311.2:c.367+308T>C NP_001298240.1:n.367+308T>C
NM_206824.3:c.174-1133T>C NP_996560.1:n.174-1133T>C